Evidence map›Paper›PMID 42221078›Full record

SynthesisFrontiers in medicine2026

Stabilized adaptive states in microbiome-human integrated physiology: reframing health and chronic disease as symbiotic biological states.

João Francisco Pollo Gaspary, Luis Felipe Dias Lopes, Fernanda Peron Gaspary, Eduarda Grando Lopes, Alfred Lee Edgar, Eduardo Poletti Camara, Antonio Geraldo Camara

Abstract readSystematic Review
In one paragraph

Synthesis in Frontiers in medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

João Francisco Pollo GasparyInstitute AuBento - Center for Education, Clinical Practice, and Research in Orthomolecular and Integrative Medicine, Santa Maria, Brazil.
Luis Felipe Dias LopesPostgraduate Program in Administration and Accounting, Center for Social and Human Sciences, Federal University of Santa Maria, Santa Maria, Brazil.
Fernanda Peron GasparyFranciscan University, Santa Maria, Brazil.
Eduarda Grando LopesVeterinary Medicine Course, Federal University of Santa Maria, Santa Maria, Brazil.
Alfred Lee EdgarDepartment of Research and Development, ElastroCrete, LLC, Veyo, UT, United States.
Eduardo Poletti CamaraInstitute Camara - Center for Clinical and Orthomolecular Practice, Ribeirão Preto, Brazil.
Antonio Geraldo CamaraInstitute Camara - Center for Clinical and Orthomolecular Practice, Ribeirão Preto, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Modern medicine has achieved remarkable precision in identifying molecular mechanisms and developing targeted interventions. However, a persistent clinical paradox remains: many chronic conditions-including metabolic, autoimmune, neuropsychiatric, and oncological disorders-exhibit long-term stability, resistance to guideline-concordant treatment, and recurrent trajectories. Despite extensive mechanistic characterization, the organizational basis of this stability remains insufficiently explained. Conceptual gap: In acute contexts such as infection and environmental intoxication, organisms can remain internally coherent while temporarily prioritizing non-host biological demands. This state-based perspective, however, has rarely been extended to chronic disease. At the same time, microbiome research has demonstrated that human physiology operates within a multigenomic system, in which exogenous gene repertoires contribute substantial metabolic and signaling capacity. Epigenetic research further indicates that repeated ecological exposures can progressively stabilize adaptive biological states over time. Proposed framework: We propose a conceptual framework in which health and disease are interpreted as stabilized adaptive states emerging from hierarchical signal integration within a multigenomic human system. In this model, chronic pathology reflects coherent but constrained regulatory configurations, rather than simple dysregulation or isolated system failure. Central to this interpretation is membrane-level decisional architecture, which governs signal routing, threshold modulation, and downstream transcriptional responses across tissues. Implications: This framework reorganizes existing evidence into a systems-level interpretation of chronic disease stability, providing a basis for generating testable hypotheses regarding state transitions, responsiveness to perturbation, and restoration of physiological flexibility. Rather than introducing new therapeutic doctrines, the model aims to clarify how biological systems stabilize over time and how such stabilization may be investigated within existing experimental paradigms. Systematic review registration: https://www.crd.york.ac.uk/PROSPERO/view/CRD420261295889, CRD420261295889; https://www.crd.york.ac.uk/PROSPERO/view/CRD420261295945, CRD420261295945.

Indexed as

adaptive stateschronic disease stabilitymembrane-level signal integrationmicrobiome–host interactionmultigenomic physiologysystems physiology

Identifiers

PMID42221078
PMCPMC13216002

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.